A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193638



Internal ID20760678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:60595870..60646001hg38UCSC Ensembl
chr18:58263103..58313234hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3850132
hg1950132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193638
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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